Canonical Allele Identifier: CA372787629

Gene: VLDLR

Linked Data

• dbSNP Id: rs1817561491
• gnomAD v4: 9-2635492-C-G
• MyVariant Identifiers: chr9:g.2635492C>G (hg19) ; chr9:g.2635492C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2635492C>G , CM000671.2:g.2635492C>G	GRCh38
NC_000009.11:g.2635492C>G , CM000671.1:g.2635492C>G	GRCh37
NC_000009.10:g.2625492C>G	NCBI36
NG_012741.1:g.18700C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382096.6:c.122C>G	ENSP00000371528.2:p.Thr41Arg
ENST00000382100.8:c.122C>G MANE Select	ENSP00000371532.2:p.Thr41Arg
ENST00000679851.1:n.107C>G
ENST00000680021.1:n.322C>G
ENST00000680243.1:c.122C>G	ENSP00000505911.1:p.Thr41Arg
ENST00000680746.1:c.122C>G	ENSP00000505030.1:p.Thr41Arg
ENST00000680891.1:c.220C>G	ENSP00000505167.1:p.Gln74Glu
ENST00000681306.1:c.122C>G	ENSP00000506072.1:p.Thr41Arg
ENST00000681618.1:c.122C>G	ENSP00000505773.1:p.Thr41Arg
ENST00000681644.1:c.220C>G	ENSP00000505180.1:p.Gln74Glu
ENST00000681770.1:n.110C>G
ENST00000681806.1:c.122C>G	ENSP00000505282.1:p.Thr41Arg
ENST00000382096.5:c.122C>G	ENSP00000371528.1:p.Thr41Arg
ENST00000382099.2:c.122C>G	ENSP00000371531.2:p.Thr41Arg
ENST00000382100.7:c.122C>G	ENSP00000371532.2:p.Thr41Arg
NM_001018056.1:c.122C>G	NP_001018066.1:p.Thr41Arg
NM_003383.3:c.122C>G	NP_003374.3:p.Thr41Arg
XM_011518029.1:c.122C>G	XP_011516331.1:p.Thr41Arg
NM_001018056.2:c.122C>G	NP_001018066.1:p.Thr41Arg
NM_001322225.1:c.122C>G	NP_001309154.1:p.Thr41Arg
NM_001322226.1:c.122C>G	NP_001309155.1:p.Thr41Arg
NM_003383.4:c.122C>G	NP_003374.3:p.Thr41Arg
XR_001746373.2:n.526C>G
XR_002956805.1:n.526C>G
NM_003383.5:c.122C>G MANE Select	NP_003374.3:p.Thr41Arg
NM_001018056.3:c.122C>G	NP_001018066.1:p.Thr41Arg
NM_001322225.2:c.122C>G	NP_001309154.1:p.Thr41Arg
NM_001322226.2:c.122C>G	NP_001309155.1:p.Thr41Arg